| Product NDC: | 59365-5030 |
| Proprietary Name: | TRIMO SAN |
| Non Proprietary Name: | Hydroxyquinoline Sulfate Sodium Lauryl Sulfate |
| Active Ingredient(s): | .25; .01 g/g; g/g & nbsp; Hydroxyquinoline Sulfate Sodium Lauryl Sulfate |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | JELLY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 59365-5030 |
| Labeler Name: | CooperSurgical, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19770401 |
| Package NDC: | 59365-5030-0 |
| Package Description: | 113.4 g in 1 TUBE (59365-5030-0) |
| NDC Code | 59365-5030-0 |
| Proprietary Name | TRIMO SAN |
| Package Description | 113.4 g in 1 TUBE (59365-5030-0) |
| Product NDC | 59365-5030 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydroxyquinoline Sulfate Sodium Lauryl Sulfate |
| Dosage Form Name | JELLY |
| Route Name | VAGINAL |
| Start Marketing Date | 19770401 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | CooperSurgical, Inc. |
| Substance Name | OXYQUINOLINE SULFATE; SODIUM LAURYL SULFATE |
| Strength Number | .25; .01 |
| Strength Unit | g/g; g/g |
| Pharmaceutical Classes |